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PROBE REFILL KIT

Page Type
Cleared 510(K)
510(k) Number
K911073
510(k) Type
Traditional
Applicant
INTERSPEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/1991
Days to Decision
87 days

PROBE REFILL KIT

Page Type
Cleared 510(K)
510(k) Number
K911073
510(k) Type
Traditional
Applicant
INTERSPEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/1991
Days to Decision
87 days